Unknown

Dataset Information

0

Straightforward Access to Multifunctional π-Conjugated P-Heterocycles Featuring an Internal Ylidic Bond.


ABSTRACT: We report the straightforward one-pot synthesis of novel 5- or 6-membered P-heterocycles featuring an internal ylidic bond: P-containing acenaphthylenes and phenanthrenes. The stability of the compounds tolerates post-functionalization through direct arylation to introduce electron-rich/poor substituents and the synthetic strategy is also compatible with the preparation of more elaborate polyaromatic scaffolds such as acenes and helicenes. Using a joint experimental (X-ray analysis, optical and redox properties) and theoretical approach, we perform a full structure-property relationships study on these new platforms. In particular, we show that molecular engineering allows not only tuning their absorption/emission across the entire visible range but also endowing them with chiroptical or non-linear optical properties, making them valuable dyes for a large panel of photonic or opto-electronic applications.

SUBMITTER: Delouche T 

PROVIDER: S-EPMC9400969 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

altmetric image

Publications

Straightforward Access to Multifunctional π-Conjugated P-Heterocycles Featuring an Internal Ylidic Bond.

Delouche Thomas T   Caytan Elsa E   Cordier Marie M   Roisnel Thierry T   Taupier Grégory G   Molard Yann Y   Vanthuyne Nicolas N   Le Guennic Boris B   Hissler Muriel M   Jacquemin Denis D   Bouit Pierre-Antoine PA  

Angewandte Chemie (International ed. in English) 20220623 31


We report the straightforward one-pot synthesis of novel 5- or 6-membered P-heterocycles featuring an internal ylidic bond: P-containing acenaphthylenes and phenanthrenes. The stability of the compounds tolerates post-functionalization through direct arylation to introduce electron-rich/poor substituents and the synthetic strategy is also compatible with the preparation of more elaborate polyaromatic scaffolds such as acenes and helicenes. Using a joint experimental (X-ray analysis, optical and  ...[more]

Similar Datasets

| S-EPMC10076471 | biostudies-literature
| S-EPMC12150314 | biostudies-literature
| S-EPMC8595307 | biostudies-literature
| S-EPMC7419521 | biostudies-literature
| S-EPMC5994875 | biostudies-literature
| S-EPMC6790668 | biostudies-literature
| S-EPMC8022320 | biostudies-literature